Associate Director/Director - Global Regulatory Affairs (GRA) Global Labeling

at  Lilly

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
Eli Lilly Cork, is made up of a talented diverse team of over 1,400 employees across 38 nationalities who deliver innovative solutions that add value across a variety of Business Service functions including Finance, Information Technology, Medical, Clinical Trials and more.
Lilly offers a premium workspace across our campus in Little Island, complete with flexible hybrid working options, healthcare, pension and life assurance benefits, subsidised canteen, onsite gym, travel subsidies and on-site parking. Inhouse People Development services, Educational Assistance, and our ‘Live Your BEST Life’ wellbeing initiatives are just some of the holistic benefits that enhance the career experience for our colleagues.
Come join our team - Be Creative, Be an Innovator, and most of all, Be Yourself!
The purpose of the Labeling role in the Global Labeling Department at Cork is to lead the development and maintenance of Core labeling documents and provide oversight of global implementation for drug and combination device products. The Associate Director leads the development of United States (US) and Canada packaging and combination device patient labeling. The Associate Director serves as the primary interface with the Printing Packaging Development (PPD) organization for implementation of US and Canada labeling. They drive consistency in labeling processes and operations.

MINIMUM QUALIFICATION REQUIREMENTS:

• Bachelor’s degree in a scientific or health sciences discipline (or equivalent experience).
• Industry-related experience in regulatory affairs and/or drug development experience for minimum of 5-8 years.